Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations

A simple, rapid, and extractive spectrophotometric methods was developed for the determination of some postsynaptic α-1 adrenoreceptor antagonist; doxazosin mesylate (DOX), terazosin (TRZ) and alfuzosine HCl (ALF) in pure forms and pharmaceutical formulations. The developed methods are based on...

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Main Authors: El Sheikh Ragaa, Esmail Nahla S., Gouda Ayman A., Basset Walid Abdel
Format: Article
Language:English
Published: Association of the Chemical Engineers of Serbia 2012-01-01
Series:Chemical Industry and Chemical Engineering Quarterly
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/1451-9372/2012/1451-93721100060E.pdf
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spelling doaj-8dd477139ceb4ed190cfd9bb01ebf73d2020-11-24T20:41:31ZengAssociation of the Chemical Engineers of SerbiaChemical Industry and Chemical Engineering Quarterly1451-93722217-74342012-01-0118217919110.2298/CICEQ110917060EExtractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulationsEl Sheikh RagaaEsmail Nahla S.Gouda Ayman A.Basset Walid AbdelA simple, rapid, and extractive spectrophotometric methods was developed for the determination of some postsynaptic α-1 adrenoreceptor antagonist; doxazosin mesylate (DOX), terazosin (TRZ) and alfuzosine HCl (ALF) in pure forms and pharmaceutical formulations. The developed methods are based on the formation of yellow colored chloroform ion-pair complexes between the basic nitrogen of the drugs and dyes, namely; bromocresol green (BCG), bromothymol blue (BTB), methyl orange (MO) and alizarine red S (ARS), in acidic buffer of pH range (3.0-5.0). The formed complexes were extracted with chloroform or dichloromethane and measured at 418, 414, 425 and 426 nm for DOX and at 419, 415, 425 and 428 for TRZ and at 418, 412, 421 and 427 nm for ALF using BCG, BTB, MO and ARS, respectively. The analytical parameters and their effects on the reported systems are investigated. Beer’s law was obeyed in the range 1.0-130 μg mL−1 with correlation coefficient (n = 6) ≥ 0.9991. The molar absorpitivity, Sandell sensitivity, detection and quantification limits were also calculated. The composition of the ion associates was found 1:1 by Job’s method. The proposed methods have been applied successfully for the analysis of the studied drugs in pure forms and in pharmaceutical formulations with percentage recoveries ranges from 99.18-100.61. The results of analysis were validated statistically. The results were in good agreement and compared with those obtained with reported methods.http://www.doiserbia.nb.rs/img/doi/1451-9372/2012/1451-93721100060E.pdfdoxazosin mesylateterazosinalfuzosine HClspectrophotometryion pair complexacid dyespharmaceutical formulations
collection DOAJ
language English
format Article
sources DOAJ
author El Sheikh Ragaa
Esmail Nahla S.
Gouda Ayman A.
Basset Walid Abdel
spellingShingle El Sheikh Ragaa
Esmail Nahla S.
Gouda Ayman A.
Basset Walid Abdel
Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
Chemical Industry and Chemical Engineering Quarterly
doxazosin mesylate
terazosin
alfuzosine HCl
spectrophotometry
ion pair complex
acid dyes
pharmaceutical formulations
author_facet El Sheikh Ragaa
Esmail Nahla S.
Gouda Ayman A.
Basset Walid Abdel
author_sort El Sheikh Ragaa
title Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
title_short Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
title_full Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
title_fullStr Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
title_full_unstemmed Extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
title_sort extractive spectrophotometric determination of some α-adrenergic-antagonists in pure forms and in pharmaceutical formulations
publisher Association of the Chemical Engineers of Serbia
series Chemical Industry and Chemical Engineering Quarterly
issn 1451-9372
2217-7434
publishDate 2012-01-01
description A simple, rapid, and extractive spectrophotometric methods was developed for the determination of some postsynaptic α-1 adrenoreceptor antagonist; doxazosin mesylate (DOX), terazosin (TRZ) and alfuzosine HCl (ALF) in pure forms and pharmaceutical formulations. The developed methods are based on the formation of yellow colored chloroform ion-pair complexes between the basic nitrogen of the drugs and dyes, namely; bromocresol green (BCG), bromothymol blue (BTB), methyl orange (MO) and alizarine red S (ARS), in acidic buffer of pH range (3.0-5.0). The formed complexes were extracted with chloroform or dichloromethane and measured at 418, 414, 425 and 426 nm for DOX and at 419, 415, 425 and 428 for TRZ and at 418, 412, 421 and 427 nm for ALF using BCG, BTB, MO and ARS, respectively. The analytical parameters and their effects on the reported systems are investigated. Beer’s law was obeyed in the range 1.0-130 μg mL−1 with correlation coefficient (n = 6) ≥ 0.9991. The molar absorpitivity, Sandell sensitivity, detection and quantification limits were also calculated. The composition of the ion associates was found 1:1 by Job’s method. The proposed methods have been applied successfully for the analysis of the studied drugs in pure forms and in pharmaceutical formulations with percentage recoveries ranges from 99.18-100.61. The results of analysis were validated statistically. The results were in good agreement and compared with those obtained with reported methods.
topic doxazosin mesylate
terazosin
alfuzosine HCl
spectrophotometry
ion pair complex
acid dyes
pharmaceutical formulations
url http://www.doiserbia.nb.rs/img/doi/1451-9372/2012/1451-93721100060E.pdf
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AT goudaaymana extractivespectrophotometricdeterminationofsomeaadrenergicantagonistsinpureformsandinpharmaceuticalformulations
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